At European level, it has been considered necessary to establish a new solid, transparent, predictable and sustainable regulatory framework for in vitro diagnostic medical devices, that guarantees the highest level of safety and protection of patients and users health, and at the same time promotes innovation and the interests of small and medium-sized enterprises that carry out their activities in this sector.
On December 27, 2022, the Royal Decree 1055/2022 on packaging and packaging waste (RDERE) was approved in
At Asphalion we count with Lead Auditors with an extensive track record and experience in the annual review of the QMS suitability and efficiency.
The new fees will not come into effect until next June, so that the fees established on December 2022 remain still valid.
Una representación de expertos de Asphalion acudió anoche a la tradicional cena de Navidad de la Sección
xEVMPD management is the Extended Eudravigilance Medicinal Product Dictionary of the European Medicinal Agency (EMA), which defines controlled vocabulary to be used for the marketing authorisation of medicinal products.
📆 13-14 October, 2022 💻 Online course ASPHALION expert André Mota, together with other
Nuestros expertos Nuria García, Regulatory Affairs Manager, y Laura Mendieta, Senior Scientific and Regulatory Affairs Officer Project
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